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Results: 1-9 |
Results: 9
Comment on: Twin pregnancy in a rudimentary uterine horn diagnosed by ultrasound and managed laparoscopically before rupture
Authors: Anwar, K Chin, KAJ
Citation: K. Anwar et Kaj. Chin, Comment on: Twin pregnancy in a rudimentary uterine horn diagnosed by ultrasound and managed laparoscopically before rupture, GYNAEC ENDO, 10(4), 2001, pp. 273-273
A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family
Authors: Hameed, A Khaliq, S Ismail, M Anwar, K Mehdi, SQ Bessant, D Payne, AM Bhattacharya, SS
Citation: A. Hameed et al., A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family, INV OPHTH V, 42(7), 2001, pp. 1436-1438
Locus for autosomal recessive nonsyndromic persistent hyperplastic primaryvitreous
Authors: Khaliq, S Hameed, A Ismail, M Anwar, K Leroy, B Payne, AA Bhattacharya, SS Mehdi, SQ
Citation: S. Khaliq et al., Locus for autosomal recessive nonsyndromic persistent hyperplastic primaryvitreous, INV OPHTH V, 42(10), 2001, pp. 2225-2228
Patient access to their records: rights or risks?
Authors: Anwar, K O' Mahony, F
Citation: K. Anwar et F. O' Mahony, Patient access to their records: rights or risks?, BR J OBST G, 107(1), 2000, pp. 141-142
A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13
Authors: Hameed, A Khaliq, S Ismail, M Anwar, K Ebenezer, ND Jordan, T Mehdi, SQ Payne, AM Bhattacharya, SS
Citation: A. Hameed et al., A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13, INV OPHTH V, 41(3), 2000, pp. 629-633
Novel locus for autosomal recessive cone-rod dystrophy CORDS mapping to chromosome 1q12-q24
Authors: Khaliq, S Hameed, A Ismail, M Anwar, K Leroy, BP Mehdi, SQ Payne, AM Bhattacharya, SS
Citation: S. Khaliq et al., Novel locus for autosomal recessive cone-rod dystrophy CORDS mapping to chromosome 1q12-q24, INV OPHTH V, 41(12), 2000, pp. 3709-3712
Glutathione-S-transferase as a selective inhibitor of oncogenic ras-p21-induced mitogenic signaling through blockade of activation of jun by jun-N-terminal kinase
Authors: Villafania, A Anwar, K Amar, S Chie, L Way, D Chung, DL Adler, V Ronai, Z Brandt-Rauf, PW Yamaizumii, Z Kung, HF Pincus, MR
Citation: A. Villafania et al., Glutathione-S-transferase as a selective inhibitor of oncogenic ras-p21-induced mitogenic signaling through blockade of activation of jun by jun-N-terminal kinase, ANN CLIN L, 30(1), 2000, pp. 57-64
Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin
Authors: Berry, V Mackay, D Khaliq, S Francis, PJ Hameed, A Anwar, K Mehdi, SQ Newbold, RJ Ionides, A Shiels, A Moore, T Bhattacharya, SS
Citation: V. Berry et al., Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin, HUM GENET, 105(1-2), 1999, pp. 168-170
Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32
Authors: Bessant, DAR Anwar, K Khaliq, S Hameed, A Ismail, M Payne, AM Mehdi, SQ Bhattacharya, SS
Citation: Dar. Bessant et al., Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32, BR J OPHTH, 83(8), 1999, pp. 919-922
Risultati: 1-9 |